Ganshorn Medizin Electronic GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ganshorn Medizin Electronic GmbH - FDA 510(k) Cleared Devices
Recent clearances: PowerCube+ Series (PowerCube Body+)
2
Total
2
Cleared
0
Denied
Ganshorn Medizin Electronic GmbH has 2 FDA 510(k) cleared medical devices. Based in Niederlauer, DE.
Latest FDA clearance: Dec 2024. Active since 2016. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Ganshorn Medizin Electronic GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ganshorn Medizin Electronic GmbH
2 devices